Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001006946.1 | 1250 | Missense Mutation | CCC,TCC | P287S | NP_001006947.1 |
NM_002997.4 | 1250 | Missense Mutation | CCC,TCC | P287S | NP_002988.3 |
XM_005262620.4 | 1250 | Missense Mutation | CCC,TCC | P311S | XP_005262677.1 |
XM_005262621.3 | 1250 | Missense Mutation | CCC,TCC | P282S | XP_005262678.3 |
XM_005262622.2 | 1250 | Missense Mutation | CCC,TCC | P269S | XP_005262679.1 |